Tzakis Andreas G, Tryphonopoulos Panagiotis, Kato Tomoaki, Nishida Seigo, Levi David M, Madariaga Juan R, Gaynor Jeffrey J, De Faria Werviston, Regev Arie, Esquenazi Violet, Weppler Debbie, Ruiz Phillip, Miller Joshua
Department of Surgery, Division of Transplantation, University of Miami School of Medicine, Miami, Florida 33136, USA.
Transplantation. 2004 Apr 27;77(8):1209-14. doi: 10.1097/01.tp.0000116562.15920.43.
The administration of alemtuzumab (Campath-1H [C1H]; Berlex Laboratories, Montville, NJ) at transplantation prevents a vigorous immune response and is believed to allow a gradual engagement of the host immune system. We report our preliminary experience with C1H and tacrolimus (Tac) immunosuppression in adult liver transplantation.
We administered C1H and low-dose Tac to 40 adult recipients of cadaveric liver allografts between December 2001 and April 2003. A control group who met the same eligibility criteria consisted of 50 liver transplant recipients treated with our standard Tac and steroids protocol.
Baseline characteristics and patient and graft survival were similar (P >0.15). The incidence of acute rejection was significantly lower during the first 2 months posttransplantation (P =0.002) and slightly lower overall in the study group versus the control group at 12 months (46% vs. 55%, P =0.12, log-rank test). Median time to rejection among those experiencing rejection was significantly longer in the study group versus control group (2.76 vs. 0.34 months, P =0.0007). The mean Tac dose, 12-hr trough level, and percentage of patients receiving maintenance steroids were significantly lower in the group receiving C1H and Tac (P <0.0001 during the first 3 months, P <0.05 thereafter), as were the mean creatinine levels (P <0.05) and incidence of nephrotoxicity (P =0.004, conversion from Tac to other agents). Finally, in the group receiving C1H/Tac, patients with an average Tac trough level less than 6.5 ng/mL during the first 2 months post-transplantation demonstrated a significantly higher rejection rate beyond that time (P =0.02).
C1H and low-dose Tac seems to be at least as effective as our standard Tac and steroids regimen in preventing acute rejection in adult liver allotransplantation with less renal toxicity and less use of maintenance steroids.
在移植时给予阿仑单抗(Campath-1H [C1H];Berlex Laboratories,新泽西州蒙特维尔)可预防强烈的免疫反应,并被认为能使宿主免疫系统逐渐参与其中。我们报告了我们在成人肝移植中使用C1H和他克莫司(Tac)免疫抑制的初步经验。
在2001年12月至2003年4月期间,我们对40例接受尸体肝同种异体移植的成年受者给予了C1H和低剂量Tac。一个符合相同入选标准的对照组由50例接受我们标准Tac和类固醇方案治疗的肝移植受者组成。
基线特征以及患者和移植物存活率相似(P>0.15)。移植后前2个月急性排斥反应的发生率显著较低(P = 0.002),并且在12个月时研究组总体上略低于对照组(46%对55%,P = 0.12,对数秩检验)。在发生排斥反应的患者中,研究组的排斥反应中位时间显著长于对照组(2.76对0.34个月,P = 0.0007)。接受C1H和Tac的组中,平均Tac剂量、12小时谷浓度以及接受维持类固醇治疗的患者百分比显著较低(前3个月P < 0.0001,此后P < 0.05),平均肌酐水平(P < 0.05)和肾毒性发生率(P = 0.004,从Tac转换为其他药物)也是如此。最后,在接受C1H/Tac的组中,移植后前2个月平均Tac谷浓度低于6.5 ng/mL的患者在该时间之后的排斥反应率显著更高(P = 0.02)。
在预防成人肝同种异体移植中的急性排斥反应方面,C1H和低剂量Tac似乎至少与我们的标准Tac和类固醇方案一样有效,且肾毒性较小,维持类固醇的使用较少。